Hostname: page-component-cd9895bd7-8ctnn Total loading time: 0 Render date: 2024-12-27T10:43:25.642Z Has data issue: false hasContentIssue false

Calcificación de los ganglios basales y psicosis en el síndrome de eliminación 22q11.2

Published online by Cambridge University Press:  12 May 2020

M. Sieberer
Affiliation:
Departamento de Psiquiatría Social y Psicoterapia, Escuela de Medicina de Hannover, Carl-Neuberg-Strasse 1, 30625Hannover, Alemania
H. Haltenhof
Affiliation:
Departamento de Psiquiatría Social y Psicoterapia, Escuela de Medicina de Hannover, Carl-Neuberg-Strasse 1, 30625Hannover, Alemania
B. Haubitz
Affiliation:
Departamento de Neurorradiología, Escuela de Medicina de Hannover, Hannover, Alemania
B. Pabst
Affiliation:
Departamento de Genética Humana, Escuela de Medicina de Hannover, Hannover, Alemania
K. Miller
Affiliation:
Departamento de Genética Humana, Escuela de Medicina de Hannover, Hannover, Alemania
P. Garlipp
Affiliation:
Departamento de Psiquiatría Social y Psicoterapia, Escuela de Medicina de Hannover, Carl-Neuberg-Strasse 1, 30625Hannover, Alemania
Get access

Resumen

Las calcificaciones cerebrales son un síntoma facultativo de hipoparatiroidismo en el síndrome de eliminación 22q11.2 (22qDS). Describimos a una paciente con 22qDS, calcificación de los ganglios basales (CGB) y síntomas psicóticos y analizamos la conexión etiológica de la CGB con los síntomas psiquiátricos. Trabajos futuros tienen que determinar la prevalencia de la CGB en el 22qDS y los trastornos psiquiátricos.

Type
Comunicación breve
Copyright
Copyright © European Psychiatric Association 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bibliografía

[1]Chow, EWCMikulis, DJZiparsky, RBScutt, LEWeksberg, RBassett, ASQualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biol Psychiatry 1999;46(10): 1436–42.CrossRefGoogle Scholar
[2]Cummings, JLGosenfeld, LFHoulihan, JPMccaffrey, TNeuropsychiatric disturbances associated with idiopathic calcification of the basal ganglio. Biol Psychiatry 1983; 18(5):591601.Google Scholar
[3]Eliez, SBarnea-Goraly, NSchmitt, JELiu, YReiss, ALIncreased basal ganglio volumes in velo-cardio-facial syndrome (deletion 22ql 1.2). Biol Psychiatry 2002;52(l):6870.CrossRefGoogle Scholar
[4]Eliez, SBlasey, CMSchmitt, EJWhite, CDHu, DReiss, ALVelocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia? Am J Psychiatry 2001; 158(3):447–53CrossRefGoogle Scholar
[5]Flint, JGoldstein, LHFamilial calcification of the basal ganglio: a case-report and review of the literature. Psychol Med 1992;22(3):581–95.CrossRefGoogle Scholar
[6]Horowitz, AShifman, SRivalin, NPisante, ADarvasi, AA survey of the 22ql 1 microdeletion in a large cohort of schizophrenia patients. Schizophr Res 2005;73:263–7.CrossRefGoogle Scholar
[7]Murphy, KCSchizophrenia and velocardio-facial syndrome. Lancet 2002;359:426–30.CrossRefGoogle Scholar
[8]Murphy, KCJones, LAOwen, MJHigh rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 1999;56:940–5.CrossRefGoogle ScholarPubMed
[9]Óskarsdóttir, SVujic, MFasth, AIncidence and prevalence of the 22ql 1 deletion syndrome: a population-based study in Western Sweden. Arch Dis Child 2004;89:148–52.CrossRefGoogle Scholar
[10]Sciré, GDallapiccola, BIannetti, PBonaiuto, FGalasso, CMingarelli, R et al. Hypoparathyroidism as the major manifestation in two patients with 22ql 1 deletions. Am J Med Genet 1994;52(4):478–82.CrossRefGoogle Scholar
[11]Shprintzen, RJGoldberg, RGolding-Kushner, KJMarion, RWLateonset psychosis in the velo-cardio-facial syndrome. Am J Med Genet 1992;42(1): 141–2.CrossRefGoogle Scholar
[12]Shprintzen, RJGoldberg, RBLewin, MLSidoti, EJBerkman, MDArgamaso, RV et al. A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardiofacial syndrome. Cleft Palate J 1978;15(1):5662.Google Scholar
[13]Simon, TJDing, LBish, JPMcDonnald-McGinn, DMZackai, EHGee, JVolumetric, connective, and morphologic changes in the brains of children with chormosome 22ql 1.2 deletion syndrome: an integrative study. Neuroimage 2005;25:169–80.CrossRefGoogle Scholar
[14]Van Amelsvoort, TDaly, EHenry, JRobertson, DNg, VOwen, M et al. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia. Arch Gen Psychiatry 2004;61:1085–96.CrossRefGoogle ScholarPubMed
[15]Van Amelsvoort, TDaly, ERobertson, DSuckling, JNg, VCritchley, H et al. Structural brain abnormalities associated with deletion at chromosome 22q 11 quantitative neuroimaging study of adults with velo-cardio-facial syndrome. Br J Psychiatry 2001;178:412–9.CrossRefGoogle Scholar
[16]Wilson, DIBurn, JScambler, PGoodship, JDiGeorge syndrome: part of CATCH 22. J Med Genet 1993;30(10):852–6.CrossRefGoogle ScholarPubMed